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Dedicated Staff

Clinical Research Associate Team

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Myriam Alexandre

💡 Clinical Research Manager

📞 +352 26970-855

📧 Myriam.Alexandre@lih.lu

Biography

Myriam Alexandre joined LIH in January 2013, as Senior Clinical Research Associate after 10 years of experience in different Clinical Research Organizations. She gained experience in supporting investigators in the conduct of clinical trials developed by pharmaceutical companies or by clinical investigators.  Appointed Clinical Research Manager in 2015, she now develops and coordinates the activities of a team composed of Clinical Research Associates to conduct clinical trials and epidemiological studies.
She also actively supports the Head of unit in the management of the unit (budget supervision, staff allocation) and the development of the unit through regular contacts with the different clinical research actors (Hospitals, Authorities, pharmaceutical companies, IBBL…) 

Main activities

• Promotion and support of local projects, support to research teams to consolidate experimental findings through quality-assured clinical research involving patients and healthy individuals
• Coordination of the clinical phase of the Personalized Functional Profiling (PFP) program: Pilot study to explore the Integrated Personalized Functional Profiling (PFP) for cancer patients with metastatic gastrointestinal cancer (mGIC) or recurrent glioblastoma (rGBM) in Luxembourg. Based on recent improvements in cancer biopsy-derived 3D-culture technologies the PFP process will screen patient derived cells (PDCs) with FDA/EMA-approved drugs to generate personalized functional response profiles. The selected drug through PFP technology will provide personalized treatment recommendation for the patient.
• Promotion of clinical research in Luxembourg
• CRA Team Supervision and Management

 

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Charlotte Lieunard

💡 Clinical Research Associate & Quality Assurance

📞 +352 26970-847

📧 Charlotte.Lieunard@lih.lu

Biography

Charlotte Lieunard joined the Clinical and Epidemiological Investigation Center in February 2009 as Clinical Research Associate. She provides support to investigator/researcher in the conduct of clinical trials: during the study start-up phase with the preparation of study documents (protocol, ICF, ...) and the management of all authorizations, during the conduct of the study with the management of patient data, study documents, and regulatory aspects, and finally during the end of the study with the closure and archiving.

Charlotte is actively involved in the organization and coordination of the unit:
• Management of the quality system of the CIEC to ensure the safety of the participants and the conduct of the projects in accordance with the Good Clinical Practice
• Key contact person for all regulatory questions and assisting LIH investigators in the submission of their projects to authorities in respect of the applicable laws and regulations
• In close collaboration with the data protection officer, Charlotte is highly involved in the implementation of the GDPR to ensure the confidentiality and protection of personal data.

Main activities

• Quality: development of new internal processes, writing and review of standards operating procedures, conduct internal audits
• Protection of personal data: point of contact at CIEC for questions regarding protection of personal data and the update of the LIH registry
• Regulatory aspects: point of contact for the review and submission of LIH projects to Competent Authorities
• Development of clinical trials at Centre François Baclesse

 

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Gloria Montanes

💡 Clinical Research Associate

📞 +352 26970-757

📧 Gloria.Montanes@lih.lu

 

Biography

Gloria received two master degrees (Human Molecular Biology  and  European Master in Biomedicine) in the University of Barcelona (UB).
She worked in basic research in the Hospital Clinic de Barcelona and afterwards she decided to move to Brussels where she started her experience in the Clinical Research field, first as Data Integration Specialist in a CRO, and afterwards as International Clinical Data Manager and International Clinical Research Associate at the European Organization for Research and Treatment of Cancer (EORTC). These experiences allowed her to obtain a strong know-how both at the scientific and the administrative level of clinical research.

Main activities

• Coordination of clinical trials from the feasibility to the closure in several research areas
• Collaboration  in the writing and review of SOPs, templates and other quality assurance documents
• Regulatory review of LIH projects
• Monitoring of clinical trials

 

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Lamia Skhiri, PhD

💡 Clinical Research Associate

📞 +352 26970-815

📧 Lamia.Skhiri@lih.lu

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Lucile Pernot, PhD

💡 Clinical Research Associate

📞 +352 26970-811

📧 Lucile.Pernot@lih.lu

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Myriam Menster

💡 Data Manager

📞 +352 26970-802

📧 Myriam.Menster@lih.lu

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Nassera Aouali, PhD

💡 Clinical Research Associate

📞 +352 26970-278

📧 Nassera.Aouali@lih.lu​

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Christelle Bahlawane, PhD

💡 Clinical Research Associate

📞 +352 26970-774

📧 Christelle.Bahlawane@lih.lu​

 

 

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